Evidence map›Paper›PMID 34518365›Full record

ArticleeNeuro

Glycogen Synthase Kinase 3 Regulates the Genesis of Displaced Retinal Ganglion Cells3.

Elena Kisseleff, Robin J Vigouroux, Catherine Hottin, Sophie Lourdel, Leah Thomas, Parth Shah, Alain Chédotal, Muriel Perron, Anand Swaroop, Jerome E Roger

Open access · goldAbstract read
In one paragraph

Article in eNeuro. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Deletion of histone demethylaseFrontiers in cellular neuroscience · 2023
    Article
  5. Review
  6. Establishing the ground squirrel as a superb model for retinal ganglion cell disorders and optic neuropathies.Laboratory investigation; a journal of technical methods and pathology · 2021
    Article
  7. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 2 countries.

Elena KisseleffParis-Saclay Institute of Neuroscience, CERTO-Retina France, CNRS, Université Paris-Saclay, 91400, Saclay, France.
Robin J VigourouxUPMC Université Paris 06, INSERM, CNRS, Institut de la Vision, Sorbonne Universités, 75012 Paris, France.
Catherine HottinParis-Saclay Institute of Neuroscience, CERTO-Retina France, CNRS, Université Paris-Saclay, 91400, Saclay, France.
Sophie LourdelParis-Saclay Institute of Neuroscience, CERTO-Retina France, CNRS, Université Paris-Saclay, 91400, Saclay, France.
Leah ThomasParis-Saclay Institute of Neuroscience, CERTO-Retina France, CNRS, Université Paris-Saclay, 91400, Saclay, France.
Parth ShahNeurobiology-Neurodegeneration and Repair Laboratory, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892.
Alain ChédotalUPMC Université Paris 06, INSERM, CNRS, Institut de la Vision, Sorbonne Universités, 75012 Paris, France.
Muriel PerronParis-Saclay Institute of Neuroscience, CERTO-Retina France, CNRS, Université Paris-Saclay, 91400, Saclay, France jerome.roger@universite-paris-saclay.fr swaroopa@nei.nih.gov muriel.perron@universite-paris-saclay.fr.ORCID 0000-0002-1558-8236
Anand SwaroopNeurobiology-Neurodegeneration and Repair Laboratory, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892 jerome.roger@universite-paris-saclay.fr swaroopa@nei.nih.gov muriel.perron@universite-paris-saclay.fr.ORCID 0000-0002-1975-1141
Jerome E RogerParis-Saclay Institute of Neuroscience, CERTO-Retina France, CNRS, Université Paris-Saclay, 91400, Saclay, France jerome.roger@universite-paris-saclay.fr swaroopa@nei.nih.gov muriel.perron@universite-paris-saclay.fr.ORCID 0000-0002-5061-230X
Centre National de la Recherche Scientifique · FRNational Institutes of Health · US

Funding

Regulation of gene expression in the retinaZ01EY000450 · NEI · NATIONAL EYE INSTITUTE · PI SWAROOP, ANAND · 2008 to 2008
$2.4M
Intramural NIH HHS Z01 EY000450
6 · The paper itself

Abstract

Glycogen synthase kinase 3 (GSK3) proteins (GSK3α and GSK3β) are key mediators of signaling pathways, with crucial roles in coordinating fundamental biological processes during neural development. Here we show that the complete loss of GSK3 signaling in mouse retinal progenitors leads to microphthalmia with broad morphologic defects. A single wild-type allele of either

Indexed as

Glycogen Synthase Kinase 3Retinal Ganglion CellsAnimalsAxonsMiceRetinaGlycogen Synthase Kinase 3cell deathdisplaced ganglion cellsglycogen synthase kinase 3medial terminal nucleuspost-translational modificationsretinal development

Identifiers

PMID34518365
PMCPMC8496207
OpenAlexW3201230377

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.